GUDIDData
eudamed_udi Primary ID: 07640109604322

CHATTANOOGA COMPEX (UDI 07640109604322)

Manufactured by Telic, S.A.U.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CHATTANOOGA COMPEX - Primary ID 07640109604322

Device Regulatory Overview

The CHATTANOOGA COMPEX (Model/Catalog Number: 602047) is a medical device manufactured by Telic, S.A.U.. This product is indexed under FDA Product Code / Category Classification C020599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
602047
Product Code / EMDN
C020599
Device Name
Electro-gel
Database Sync Date
2026-08-09 16:51:01

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of CHATTANOOGA COMPEX?

The registered manufacturer of record for CHATTANOOGA COMPEX is Telic, S.A.U..

What is the Primary UDI-DI identifier for CHATTANOOGA COMPEX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640109604322.

What classification code is assigned to this device?

This device is registered under product classification code C020599.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint